Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g47940 A02 38622736 C T intron_variant MODIFIER c.247+1212G>A| S63
2 BAA02g47940 A02 38623154 C T intron_variant MODIFIER c.247+794G>A| S53
3 BAA02g47940 A02 38623297 G A intron_variant MODIFIER c.247+651C>T| S259
4 BAA02g47940 A02 38623704 C T intron_variant MODIFIER c.247+244G>A| S18
5 BAA02g47940 A02 38624065 G A missense_variant MODERATE c.130C>T|p.His44Tyr S62
6 BAA02g47940 A02 38624178 C T synonymous_variant LOW c.105G>A|p.Glu35Glu S260
7 BAA02g47940 A02 38625230 C T intron_variant MODIFIER c.21-968G>A| S42
8 BAA02g47940 A02 38625640 G A intron_variant MODIFIER c.21-1378C>T| S276
9 BAA02g47940 A02 38625810 A T intron_variant MODIFIER c.21-1548T>A| S55
10 BAA02g47940 A02 38625813 C T intron_variant MODIFIER c.21-1551G>A| S104
S52
11 BAA02g47940 A02 38626782 G A intron_variant MODIFIER c.21-2520C>T| S148
S210
S31
12 BAA02g47940 A02 38627056 C T intron_variant MODIFIER c.21-2794G>A| S199
13 BAA02g47940 A02 38628491 G A intron_variant MODIFIER c.21-4229C>T| S229
14 BAA02g47940 A02 38628646 C T intron_variant MODIFIER c.21-4384G>A| S194
15 BAA02g47940 A02 38628864 G A intron_variant MODIFIER c.21-4602C>T| S44
16 BAA02g47940 A02 38629214 G A intron_variant MODIFIER c.20+4889C>T| S50
17 BAA02g47940 A02 38629273 G A intron_variant MODIFIER c.20+4830C>T| S174
S27
18 BAA02g47940 A02 38629336 C T intron_variant MODIFIER c.20+4767G>A| S289
S290
19 BAA02g47940 A02 38634136 T C upstream_gene_variant MODIFIER c.-14A>G|
20 BAA02g47940 A02 38635365 C T upstream_gene_variant MODIFIER c.-1243G>A| S185
21 BAA02g47940 A02 38635533 G A upstream_gene_variant MODIFIER c.-1411C>T| S235
22 BAA02g47940 A02 38635582 C T upstream_gene_variant MODIFIER c.-1460G>A| S299
23 BAA02g47940 A02 38635650 C T upstream_gene_variant MODIFIER c.-1528G>A| S53
24 BAA02g47940 A02 38635776 G A upstream_gene_variant MODIFIER c.-1654C>T| S279